Canonical Allele Identifier: PA891855700
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 585443
ClinVar RCV Id: RCV000710628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060606.3:p.His1075Asp
CA1310223
NM_018136.5:c.3223C>G